10266 Results for "

Targeting

" in MedChemExpress (MCE) Product Catalog:
Products (10266)

10266 Results for "Targeting" in MCE Product Catalog:

21
21 Cited Publications
Cat. No.: HY-15233
CAS No.: 917389-32-3
Purity:  99.96%
Synonyms: AIC246; MK-8228
Target:  

CMV

Research Areas:  

Infection Cancer

Letermovir (AIC246) is a potent inhibitor of CMV, which targets the viral terminase complex and remains active against virus resistant to DNA polymerase inhibitors.
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20
20 Cited Publications
Cat. No.: HY-P9908
CAS No.: 331731-18-1
Synonyms: Anti-Human TNF-alpha, Human Antibody; ABBV-3373 Antibody

Target:  

TNF Receptor Bacterial

Research Areas:  

Inflammation/Immunology Cancer

Adalimumab is a human monoclonal IgG1 antibody targeting tumour necrosis factor α (TNF-α).
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19
19 Cited Publications
Cat. No.: HY-Y1750A
CAS No.: 646-03-7
Synonyms: BAPN hydrochloride
β-Aminopropionitrile (BAPN) hydrochloride is a specific, irreversible and orally active lysyl oxidase (LOX) inhibitor. β-Aminopropionitrile hydrochloride targets the active site of LOX or LOXL isoenzymes .
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19
19 Cited Publications
Cat. No.: HY-Y1750
CAS No.: 151-18-8
Synonyms: BAPN
β-Aminopropionitrile (BAPN) is a specific, irreversible and orally active lysyl oxidase (LOX) inhibitor. β-Aminopropionitrile targets the active site of LOX or LOXL isoenzymes. β-Aminopropionitrile can be used for the study of obesity .
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19
19 Cited Publications
Cat. No.: HY-N0279
CAS No.: 18956-16-6
Synonyms: Cardamomin; Alpinetin chalcone
Cardamonin can be found from cardamom, and can target various signaling molecules, transcriptional factors, cytokines and enzymes. Cardamonin can inhibit mTOR, NF-κB, Akt, STAT3, Wnt/β-catenin and COX-2. Cardamonin shows anticancer, anti-inflammatory, antimicrobial and antidiabetic activities .
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17
17 Cited Publications
Cat. No.: HY-10338
CAS No.: 849217-64-7
Purity:  99.45%
Synonyms: XL880; GSK1363089; GSK089; EXEL-2880
Target:  

VEGFR c-Met/HGFR

Research Areas:  

Cancer

Foretinib is a multi-target tyrosine kinase inhibitor with IC50s of 0.4 nM and 0.9 nM for Met and KDR.
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16
16 Cited Publications
Cat. No.: HY-102007A
CAS No.: 1131626-47-5
Purity:  99.68%
Target:  

HSP

Research Areas:  

Cancer

Gamitrinib TPP hexafluorophosphate is a Gamitrinib (GA) mitochondrial matrix inhibitor. Gamitrinib TPP hexafluorophosphate is a mitochondrial targeted HSP90 inhibitor with anti-cancer activity.
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16
16 Cited Publications
Cat. No.: HY-B1161
CAS No.: 40596-69-8
Synonyms: ZR-515
Research Areas:  

Others

Methoprene, an insect juvenile growth hormone mimic, is a growth-regulating insecticide that manifests its toxicity to target organisms by acting as a juvenile hormone agonist .
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16
16 Cited Publications
Cat. No.: HY-14422
CAS No.: 1246525-60-9
Purity:  99.75%
Target:  

ROR

Research Areas:  

Cancer

SR1078 is a selective agonist of retinoic acid receptor-related orphan receptor α/γ (RORα/RORγ). SR1078 directly binds to the ligand binding domain of RORα and RORγ and increases the transcriptional activity of these receptors, leading to stimulation of RORα/γ target gene transcription .
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14
14 Cited Publications
Cat. No.: HY-13631D
CAS No.: 1599440-33-1
Purity:  99.30%
Synonyms: Exatecan derivative for ADC
Research Areas:  

Cancer

DXd (Exatecan derivative for ADC) is a potent DNA topoisomerase I inhibitor, with an IC50 of 0.31 μM, used as a conjugated drug of HER2-targeting ADC (DS-8201a).
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14
14 Cited Publications
Cat. No.: HY-112088
CAS No.: 2057509-72-3
Purity:  99.98%
Target:  

CDK

Research Areas:  

Cancer

AZD4573 is a potent and highly selective CDK9 inhibitor (IC50 of <4 nM) that enables transient target engagement for the treatment of hematologic malignancies .
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14
14 Cited Publications
Cat. No.: HY-N2065
CAS No.: 5119-48-2
Withaferin A is a steroidal lactone isolated from Withania somnifera, inhibits NF-kB activation and targets vimentin, with potent antiinflammatory and anticancer activities. Withaferin A is an inhibitor of endothelial protein C receptor (EPCR) shedding.
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14
14 Cited Publications
Cat. No.: HY-100498A
CAS No.: 1416771-10-2
Purity:  99.89%
Target:  

FAK Apoptosis

Research Areas:  

Cancer

GSK-2256098 hydrochloride is a focal adhesion kinase (FAK) inhibitor that exhibits potential antiangiogenic and antineoplastic activities. GSK-2256098 hydrochloride targets FAK to inhibit tumor cell growth by regulating cell adhesion, migration, proliferation, and survival.
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14
14 Cited Publications
Cat. No.: HY-15729
CAS No.: 1374640-70-6
Purity:  99.79%
Synonyms: CO-1686; AVL-301; CNX-419
Target:  

EGFR

Research Areas:  

Cancer

Rociletinib (CO-1686) is an orally delivered kinase inhibitor that specifically targets the mutant forms of EGFR including T790M, and the Ki values for EGFRL858R/T790M and EGFRWT are 21.5 nM and 303.3 nM, respectively.
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14
14 Cited Publications
Cat. No.: HY-15729A
CAS No.: 1446700-26-0
Purity:  98.04%
Synonyms: CO-1686 hydrobromide; AVL-301 hydrobromide; CNX-419 hydrobromide
Target:  

EGFR

Research Areas:  

Cancer

Rociletinib hydrobromide (CO-1686 hydrobromide) is an orally delivered kinase inhibitor that specifically targets the mutant forms of EGFR including T790M, and the Ki values for EGFRL858R/T790M and EGFRWT are 21.5 nM and 303.3 nM, respectively.
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13
13 Cited Publications
Cat. No.: HY-11038D
Purity:  97.39%
Synonyms: PU-H71 formic
Target:  

HSP

Research Areas:  

Cancer

Zelavespib formic (PU-H71 formic) is a potent Hsp90 inhibitor with an IC50 value of 51 nM for Hsp90 in MDA-MB-468 cells .
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13
13 Cited Publications
Cat. No.: HY-10407
CAS No.: 215543-92-3
Purity:  99.86%
Target:  

VEGFR FGFR PDGFR

Research Areas:  

Cancer

SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGFRβ, respectively.
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13
13 Cited Publications
Cat. No.: HY-P9927
CAS No.: 1229022-83-6
Synonyms: AIN457

Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology Cancer

Secukinumab (AIN457) is a high affinity, human monoclonal antibody targeted against interleukin (IL)-17A. Secukinumab is the first-in-class anti-IL-17 agent used for the research of plaque psoriasis, ankylosing spondylitis and psoriatic arthritis .
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13
13 Cited Publications
Cat. No.: HY-10423
CAS No.: 936890-98-1
Purity:  99.95%
Synonyms: ASP7486
Target:  

mTOR Autophagy

Research Areas:  

Cancer

OSI-027 (ASP7486) is a potent, selective, orally active and ATP-competitive mTOR kinase activity inhibitor with an IC50 of 4 nM. OSI-027 targets both mTORC1 and mTORC2 with IC50s of 22 nM and 65 nM, respectively .
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13
13 Cited Publications
Cat. No.: HY-101920
CAS No.: 1644443-47-9
Purity:  99.95%
Target:  

Autophagy PI3K

Research Areas:  

Neurological Disease Cancer

Autophinib is a potent, selective autophagy inhibitor with IC50s of 90 nM and 40 nM for starvation- and Rapamycin-induced autophagy, respectively. Autophinib is also an ATP competitive Vacuolar Protein Sorting 34 (VPS34) inhibitor with an IC50 of 19 nM. Autophinib inhibits autophagy induced by starvation or Rapamycin by targeting VPS34 .
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